Amorphous body composed of heterocyclic compound, solid dispersion and pharmaceutical preparation each comprising the same, and process for production of the same
[Problems] The object is to improve the absorbability of a heterocyclic compound including s-triazine and a pyrimidine derivative in vitro. [Means for Solving Problems] Disclosed is, for example, an amorphous body of a heterocyclic compound as represented by the general formula (I) [wherein each of R's and others is as defined in the description] including s-triazine and a pyrimidine derivative, or a hydrate, a solvate or a pharmaceutically acceptable salt of the heterocyclic compound. Also disclosed is a process for producing the amorphous body. Further disclosed are: a solid dispersion comprising the amorphous body; and a medicinal preparation comprising the solid dispersion.
1. An amorphous body composed of a heterocyclic compound represented by general formula (I):
wherein, X represents a nitrogen atom or CH;
R 1 and R 2 , both or either one, represent a hydrogen atom, a hydroxyl group, a halogen, an amino group, a C 1 -C 6 alkylamino group, a C 1 -C 6 alkoxy group, a C 1 -C 6 alkyl group, or a cyano group;
R 3 represents a hydrogen atom, a difluoromethyl group, an amino group, a C 1 -C 6 alkylamino group, a methyl, or a hydroxymethyl group;
R 4 and R 5 represent a hydrogen atom or a C 1 -C 6 alkyl group; and
R 6 represents a morpholino, optionally substituted with 1 to 2 C 1 -C 6 alkyl groups, a pyrrolidinyl, optionally substituted with a hydroxy C 1 -C 6 alkyl group, a piperidino, optionally substituted with 1 to 2 oxygen atoms, a hydroxyl group, a formyl, or a C 1 -C 6 alkyl group, a piperazinyl, optionally substituted with 1 to 2 oxygen atoms, the nitrogen at position 4 optionally substituted with a substituent selected from the group consisting of formyl, hydroxyl C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, oxo C 1 -C 6 alkyl, aromatic carbonyl, benzylcarbonyl and substituted carbamoyl, or a 1,4-diazepano, optionally substituted with 1 to 2 oxygen atoms, the nitrogen at position 4 optionally substituted with a substituent selected from the group consisting of formyl, hydroxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, oxo C 1 -C 6 alkyl, aromatic carbonyl, benzyl carbonyl and substituted carbamoyl; or a hydrate thereof, a solvate thereof, or a pharmaceutically acceptable salt thereof.
2. The amorphous body according to claim 1 , produced by a spray drying method, a mixed grinding method, a fusion method or a solvent method.
3. A solid dispersion comprising the amorphous body according to claim 1 and a pharmaceutically acceptable solid polymer.
4. The solid dispersion according to claim 3 , wherein said solid polymer is a cellulose derivative.
5. The solid dispersion according to claim 4 , wherein said cellulose derivative is hydroxypropyl cellulose or hypromellose.
6. The solid dispersion according to claim 3 , wherein the mass ratio of said heterocyclic compound, the hydrate thereof, the solvate thereof, or the pharmaceutically acceptable salt thereof and said solid polymer is 1:0.1 to 1:10.
7. The solid dispersion according to claim 6 , wherein said mass ratio is 1:2 to 2.5.
8. The solid dispersion according to claim 3 , further comprising an excipient, a disintegrant and a lubricant.
9. A formulation comprising the solid dispersion according to claim 3 , provided in the form of a powder, a fine granule, a granule, a tablet or a capsule.
10. A method for producing an amorphous body composed of a heterocyclic compound represented by general formula (I):
wherein, X represents a nitrogen atom or CH;
R 1 and R 2 , both or either one, represent a hydrogen atom, a hydroxyl group, a halogen, an amino group, a C 1 -C 6 alkylamino group, a C 1 -C 6 alkoxy group, a C 1 -C 6 alkyl group, or a cyano group;
R 3 represents a hydrogen atom, a difluoromethyl group, an amino group, a C 1 -C 6 alkylamino group, a methyl, or a hydroxymethyl group;
R 4 and R 5 represent a hydrogen atom or a C 1 -C 6 alkyl group; and
R 6 represents a morpholino, optionally substituted with 1 to 2 C 1 -C 6 alkyl groups, a pyrrolidinyl, optionally substituted with a hydroxy C 1 -C 6 alkyl group, a piperidino, optionally substituted with 1 to 2 oxygen atoms, a hydroxyl group, a formyl, or a C 1 -C 6 alkyl group, piperazinyl, optionally substituted with 1 to 2 oxygen atoms, the nitrogen at position 4 optionally substituted with a substituent selected from the group consisting of formyl, hydroxyl C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, oxo C 1 -C 6 alkyl, aromatic carbonyl, benzylcarbonyl and substituted carbamoyl, or a 1,4-diazepano, optionally substituted with 1 to 2 oxygen atoms, the nitrogen at position 4 optionally substituted with a substituent selected from the group consisting of formyl, hydroxy C 1 -C 6 alkyl, C 1 -C 6 alkoxycarbonyl, oxo C 1 -C 6 alkyl, aromatic carbonyl, benzyl carbonyl and substituted carbamoyl; or a hydrate thereof, a solvate thereof, or a pharmaceutically acceptable salt thereof;
said method comprising dissolving said heterocyclic compound, the hydrate thereof, the solvate thereof or the pharmaceutically acceptable salt thereof in a solvent to prepare a feed solution;
spraying said feed solution; and
drying the sprayed feed solution to obtain said amorphous body.